M. Finbow

发表

The Effects of a Mutant Connexin 26 on Epidermal Differentiation

L. Tetley, S. Bryson, T. Aasen, 2003, Cell communication & adhesion.

The vacuolar H+-ATPase: a universal proton pump of eukaryotes.

M. Finbow, M. Harrison, 1997, The Biochemical journal.

Ductin – a proton pump component, a gap junction channel and a neurotransmitter release channel

M. Finbow, M. Harrison, P. Jones, 1995, BioEssays : news and reviews in molecular, cellular and developmental biology.

A Structural Analysis of the Gap Junctional Channel and the 16K Protein

J. Findlay, J. Keen, M. Finbow, 1990 .

Permeability of junctions between animal cells. Intercellular exchange of various metabolites and a vitamin-derived cofactor.

M. Finbow, J. Pitts, 1981, Experimental cell research.

Targeted epidermal expression of mutant Connexin 26(D66H) mimics true Vohwinkel syndrome and provides a model for the pathogenesis of dominant connexin disorders.

L. Tetley, S. Bryson, T. Aasen, 2003, Human molecular genetics.

Membrane insertion and assembly of ductin: a polytopic channel with dual orientations.

M. Finbow, P. Jones, J. Dunlop, 1995, The EMBO journal.

Connexins and the vacuolar proteolipid-like 16-kDa protein are not directly associated with each other but may be components of similar or the same gap junctional complexes.

M. Finbow, L. Meagher, 1992, Experimental cell research.

The E5 oncoprotein target: A 16‐kDa channel‐forming protein with diverse functions

R. Schlegel, J. Findlay, R. Schlegel, 1991, Molecular carcinogenesis.

Structure of a 16 kDa integral membrane protein that has identity to the putative proton channel of the vacuolar H(+)-ATPase.

E. Eliopoulos, J. Findlay, J. Keen, 1992, Protein engineering.

The functional integration of cells in animal tissues

M. Finbow, J. Pitts, 1982 .

E 5 transforming proteins of papillomaviruses do not disturb the activity of the vacuolar H M-ATPase

M. Campo, M. Finbow, L. Meagher, 2022 .

Disposition and orientation of ductin (DCCD-reactive vacuolar H(+)-ATPase subunit) in mammalian membrane complexes.

D. Apps, E. Kam, M. Finbow, 1993, Experimental cell research.

Analysis of vertebrate gap junction protein.

M. Finbow, J. Shuttleworth, J. Pitts, 1983, The EMBO journal.

Tissue and species conservation of the vertebrate and arthropod forms of the low molecular weight (16–18000) proteins of gap junctions

M. Finbow, J. Pitts, N. Lane, 1988, Cell and Tissue Research.

Independent lines of evidence suggesting a major gap junctional protein with a molecular weight of 26,000.

J. Revel, M. Finbow, R. Johnson, 1980, Proceedings of the National Academy of Sciences of the United States of America.

VERTEBRATE AND INVERTEBRATE GAP JUNCTIONS: A COMMON MOLECULAR BASIS?

M. Finbow, 1997, Cell biology international.

Interaction of inhibitors of the vacuolar H(+)-ATPase with the transmembrane Vo-sector.

J. Findlay, D. Marsh, N. Dixon, 2004, Biochemistry.

Functional properties of a hybrid vacuolar H(+)-ATPase in Saccharomyces cells expressing the Nephrops 16-kDa proteolipid.

J. Findlay, M. Finbow, M. Harrison, 1994, European journal of biochemistry.

Assembly of the yeast vacuolar H+‐ATPase and ATP hydrolysis occurs in the absence of subunit c″

M. Finbow, L. Gibson, M. Scott, 2005, FEBS letters.

Binding of human papillomavirus 16 E5 to the 16 kDa subunit c (proteolipid) of the vacuolar H+-ATPase can be dissociated from the E5-mediated epidermal growth factor receptor overactivation

A. Alonso, M. Finbow, M. Rodríguez, 2000, Oncogene.

The gap junction-like form of a vacuolar proton channel component appears not to be an artifact of isolation: an immunocytochemical localization study.

M. Finbow, B. Leitch, 1990, Experimental cell research.

The bovine papillomavirus type 4 E8 protein binds to ductin and causes loss of gap junctional intercellular communication in primary fibroblasts

M. Campo, M. Cairney, M. Finbow, 1996, Journal of virology.

E5 transforming proteins of papillomaviruses do not disturb the activity of the vacuolar H(+)-ATPase.

M. Campo, M. Finbow, L. Meagher, 2001, The Journal of general virology.

Binding of bovine papillomavirus type 4 E8 to ductin (16K proteolipid), down-regulation of gap junction intercellular communication and full cell transformation are independent events.

V. O’Brien, M. Finbow, J. Pitts, 2000, The Journal of general virology.

Polyamines regulate gap junction communication in connexin 43-expressing cells.

M. Hodgins, M. Finbow, Leonard J. Shore, 2001, The Biochemical journal.

Is the gap junction channel--the connexon--made of connexin or ductin?

M. Finbow, J. Pitts, 1993, Journal of cell science.

Inhibition of dye-coupling in Patella (Mollusca) embryos by microinjection of antiserum against nephrops (Arthropoda) gap junctions.

F. Serras, M. Finbow, T. Buultjens, 1988, Experimental cell research.

Interaction of spin-labeled inhibitors of the vacuolar H+-ATPase with the transmembrane Vo-sector.

J. Findlay, K. Väänänen, D. Marsh, 2008, Biophysical journal.

Molecular genetic analysis of V-ATPase function in Drosophila melanogaster.

K. Kaiser, J. Dow, S. Davies, 1997, The Journal of experimental biology.

The Gap Junction

J D Pitts, M. Finbow, J. Pitts, 1986, Journal of Cell Science.

Evidence for a common structure for a class of membrane channels.

J. Findlay, A. Holzenburg, D. Marsh, 1993, European journal of biochemistry.

Junctional Permeability and Its Consequences

M. Finbow, J. Pitts, 1977 .

Evidence that the 16 kDa proteolipid (subunit c) of the vacuolar H(+)-ATPase and ductin from gap junctions are the same polypeptide in Drosophila and Manduca: molecular cloning of the Vha16k gene from Drosophila.

K. Kaiser, J. Findlay, J. Keen, 1994, Journal of cell science.

Atomic force microscopy of arthropod gap junctions.

R. Lal, S. John, D. Saner, 1997, Journal of structural biology.

Molecular structure of the gap junctional channel.

E. Kam, M. Finbow, J. Pitts, 1987, Ciba Foundation symposium.

Evidence that there are two copies of subunit c" in V0 complexes in the vacuolar H+-ATPase.

M. Finbow, L. Gibson, G. Cadwallader, 2002, The Biochemical journal.

Sequence of a cDNA from Drosophila coding for the 16 kD proteolipid component of the vacuolar H(+)-ATPase.

M. Finbow, P. Mclean, L. Meagher, 1990, Nucleic acids research.

Identification of lipid-accessible sites on the nephrops 16-kDa proteolipid incorporated into a hybrid vacuolar H(+)-ATPase: site-directed labeling with N-(1-Pyrenyl)cyclohexylcarbodiimide and fluorescence quenching analysis.

J. Findlay, B. Powell, M. Finbow, 2000, Biochemistry.

Postulate for the molecular mechanism of the vacuolar H(+)-ATPase (hypothesis).

J. Findlay, M. Finbow, M. Harrison, 1997, Molecular membrane biology.

Incorporation of transmembrane peptides from the vacuolar H(+)-ATPase in phospholipid membranes: spin-label electron paramagnetic resonance and polarized infrared spectroscopy.

J. Findlay, D. Marsh, N. Dixon, 2008, Biochemistry.

Junctional communication and cellular differentiation.

E. Kam, M. Finbow, J. Pitts, 1988, The British journal of cancer. Supplement.

The morphology and coupling of Aplysia bag cells within the abdominal ganglion and in cell culture.

L. Kaczmarek, F. Strumwasser, M. Finbow, 1979, Journal of neurobiology.

Structural investigations of membrane proteins: the versatility of electron microscopy.

A. Holzenburg, R. Ford, M. Finbow, 1992, Biochemical Society Transactions.

Metabolic interactions between animal cells through permeable intercellular junctions.

J D Pitts, M. Finbow, J. Sheridan, 1979, Experimental cell research.

Junctional Communication and Communication Compartments in Development

E. Kam, M. Finbow, J. Shuttleworth, 1985 .

Interactions between normal mammary epithelial cells and mammary tumour cells in a model system

L. Quarrie, M. Finbow, J. Pitts, 1999, Cell proliferation.

Helical Interactions and Membrane Disposition of the 16-kDa Proteolipid Subunit of the Vacuolar H+-ATPase Analyzed by Cysteine Replacement Mutagenesis*

J. Findlay, M. Finbow, M. Harrison, 1999, The Journal of Biological Chemistry.

Structure of the Ductin Channel

M. Finbow, J. Pitts, Malcolm E. Finbow, 1998, Bioscience reports.

A divalent-ion binding site on the 16-kDa proton channel from Nephrops norvegicus--revealed by EPR spectroscopy.

D. Marsh, M. Finbow, T. Páli, 2006, Biochimica et biophysica acta.

Interaction of dibutyltin-3-hydroxyflavone bromide with the 16 kDa proteolipid indicates the disposition of proton translocation sites of the vacuolar ATPase.

J. Findlay, D. E. Griffiths, M. Finbow, 1996, The Biochemical journal.